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Organ Crosstalk in CKD-Associated Frailty: Mechanistic Insights, Translational Opportunities, and Clinical

Hiroshi Watanabe1, Yutaka Kitazato2, Shu Hirashima2

  • 1Department of Clinical Pharmacy and Therapeutics, Graduate School of Pharmaceutical Sciences, Kumamoto University.

Insights

Chronic kidney disease (CKD) frailty involves sarcopenia, bone fragility, and cognitive decline due to aging and systemic issues. This review proposes a unified model focusing on inter-organ communication for better CKD patient care.

Area of Science:

  • Nephrology
  • Gerontology
  • Systems Biology

Background:

  • Frailty in chronic kidney disease (CKD) is linked to accelerated aging and multisystem impairments.
  • A key feature is the triple burden: sarcopenia, bone fragility, and cognitive impairment.
  • These deficits share common drivers like uremic toxicity, inflammation, and hormonal dysregulation.

Purpose of the Study:

  • To synthesize current knowledge on CKD-associated frailty's epidemiology, diagnosis, and mechanisms.
  • To highlight the role of inter-organ crosstalk, particularly muscle-bone and muscle-brain axes.
  • To propose a unified pathophysiological model for frailty in CKD.

Main Methods:

  • Review of existing literature on CKD-associated frailty.
  • Synthesis of evidence on shared pathophysiological drivers.
  • Analysis of organ crosstalk mechanisms, focusing on skeletal muscle.

Main Results:

  • CKD frailty presents a triple burden (sarcopenia, bone fragility, cognitive impairment) driven by shared pathophysiological factors.
  • Inter-organ communication, especially via muscle-bone and muscle-brain axes, integrates these deficits.
  • Advances in biomarkers and imaging suggest a move towards network-informed care.

Conclusions:

  • CKD-related frailty is a disorder of disrupted inter-organ communication, leading to a triple burden of decline.
  • A unified model emphasizes earlier recognition and personalized, multimodal interventions.
  • Re-evaluation of CKD treatment targets is needed for frailty prevention and functional preservation.

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